A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv761e214



Internal ID22756655
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:216937927..217043218hg38UCSC Ensembl
chr2:217802650..217907941hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38105292
hg19105292
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3594300, esv3594301
SamplesNA19055, NA19917
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv761e214
Frequency
Sample Size2504
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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